RGD:127291532 Rat Genome Database

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Variant: RGD:127291532 -  Homo sapiens

RGD ID: 127291532
RS ID: rs35782983
ClinVar ID: CV1154598
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127400309  WDR1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 10,117,728
GRCh38 4 10,116,104
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005112.5:c.138+9C>T
NM_017491.5:c.138+9C>T
NG_027876.1:g.5846C>T
NC_000004.12:g.10116104G>A
More... 		11/25/2020 intron variant benign AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:WDR1
Accession:NM_017491
Location:INTRON

Gene Symbol:WDR1
Accession:NM_005112
Location:INTRON

Gene Symbol:WDR1
Accession:XM_017008880
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001510424 CLINVAR
  RCV003490269 CLINVAR
dbSNP (RS) rs35782983 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene WDR1 CLINVAR
OMIM 604734 CLINVAR